Canonical Allele Identifier: CA359721265

Gene: CCNO

Linked Data

• MyVariant Identifiers: chr5:g.54527502C>A (hg19) ; chr5:g.55231674C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55231674C>A , CM000667.2:g.55231674C>A	GRCh38
NC_000005.9:g.54527502C>A , CM000667.1:g.54527502C>A	GRCh37
NC_000005.8:g.54563259C>A	NCBI36
NG_034201.1:g.7044G>T
NG_051620.1:g.642G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.754G>T MANE Select	ENSP00000282572.4:p.Ala252Ser
ENST00000282572.4:c.754G>T	ENSP00000282572.4:p.Ala252Ser
ENST00000501463.2:c.*734G>T	ENSP00000422485.1:n.*734G>T
NM_021147.4:c.754G>T	NP_066970.3:p.Ala252Ser
NR_125346.1:n.1324G>T
NR_125347.1:n.953G>T
NR_125348.1:n.818G>T
NM_021147.5:c.754G>T MANE Select	NP_066970.3:p.Ala252Ser
NR_125346.2:n.1215G>T
NR_125347.2:n.844G>T